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Bioactivation is a metabolic process that transforms less reactive substances into highly reactive metabolites, initiating tissue toxicity. This transformation can lead to various toxic effects, including carcinogenesis and teratogenesis. Reactive metabolites are classified into two main types: electrophiles and free radicals.Electrophiles are electron-deficient species and are produced primarily by the enzyme cytochrome P-450 during the metabolism of compounds containing carbon, nitrogen, or...
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Related Experiment Video

Updated: Jul 9, 2026

Automated, Quantitative Cognitive/Behavioral Screening of Mice: For Genetics, Pharmacology, Animal Cognition and Undergraduate Instruction
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Modernizing persistence-bioaccumulation-toxicity (PBT) assessment with high throughput animal-free methods.

Beate I Escher1,2, Rolf Altenburger3, Matthias Blüher4

  • 1Helmholtz Centre for Environmental Research-UFZ, Permoserstr. 15, E04318, Leipzig, Germany. beate.escher@ufz.de.

Archives of Toxicology
|March 23, 2023
PubMed
Summary

New hazard indicators, cumulative toxicity equivalents (CTE) and persistent toxicity equivalents (PTE), offer a high-throughput, animal-free method for assessing chemical safety. These indicators streamline persistence, bioaccumulation, and toxicity evaluations, supporting sustainable chemical strategies.

Keywords:
BiodegradationHazard assessmentIn vitro bioassayMobilityNew approach methodologies (NAMs)PersistenceToxicity

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Area of Science:

  • Environmental Chemistry
  • Toxicology
  • Chemical Safety Assessment

Background:

  • Current methods for assessing chemical persistence (P), bioaccumulation (B), and toxicity (T) under regulations like REACH are complex, inefficient, and often rely on animal testing.
  • These traditional approaches can lead to inaccurate conclusions and hinder the timely evaluation of chemical safety.

Purpose of the Study:

  • To introduce novel hazard indicators, cumulative toxicity equivalents (CTE) and persistent toxicity equivalents (PTE), as replacements for existing PBT assessment methods.
  • To propose a high-throughput, in vitro-based workflow for evaluating chemical hazards, including the emerging concept of mobility (M).

Main Methods:

  • Development of two new hazard indicators: CTE (direct toxicity measurement) and PTE (toxicity after simulated environmental degradation).
  • Utilizing high-throughput in vitro bioassays to measure CTE and PTE, avoiding the need for analytical identification of transformation products or mixture components.
  • Integration of P, B/M, and T assessment into a single experimental workflow.

Main Results:

  • CTE and PTE provide a comprehensive measure of toxicity and its persistence or degradability.
  • The proposed indicators can be measured using animal-free in vitro assays, significantly reducing reliance on animal testing.
  • The methodology offers a streamlined approach to hazard assessment, applicable to single chemicals, substitution products, and mixtures.

Conclusions:

  • CTE and PTE represent a significant advancement in chemical safety assessment, offering a more efficient and ethical alternative to traditional PBT methods.
  • These indicators support the European Union's Chemicals Strategy for Sustainability by providing robust data for regulatory decision-making.
  • The proposed workflow facilitates high-throughput screening and integrates key hazard parameters, enhancing the overall safety evaluation of chemicals.